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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25795Generated: October 26, 2026

Ethoxyquin → 2,2,4-Trimethyl-1,2-dihydro-6-quinolinol

https://huagongshe.com/reaction/25795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxyquinHCID 3293—
ReactantBoron tribromideHCID 25134—
SolventDichloromethaneHCID 6344—
Product2,2,4-Trimethyl-1,2-dihydro-6-quinolinolHCID 59979945.9%

Reaction Steps

A solution of 31 g of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline in 300 mL of dichloromethane was treated with 30 mL of boron tribromide dropwise at −78° C. After the addition of boron tribromide, the cooling bath was removed and the reaction mixture was allowed to warm to room temperature. The resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was then poured into crushed ice and the pH was adjusted to 9 with sodium bicarbonate. The product was the extracted into EtOAc. The organic solution was washed with water and brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by filtering through a short plug of silica gel eluting with 25% EtOAc in hexanes solution to give 12.4 g of 2,2,4-trimethyl-1,2-dihydroquinolin-6-ol as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858627B2
Source datasetuspto-grants-2005_02
ORD IDord-b788bc3ae1e342adb325965bd12b86b8
Source noteuspto-grants-2005_02